The document on Good Regulatory Practices for regulatory oversight of medical products is under public consultation due on 11 September 2020. Please send your comments to Marie Valentin (valentinm@who.int) and Carolyn Doucelin (doucelinc@who.int).   Further information: https://www.who.int/medicines/areas/quality_safety/quality_assurance/projects/en/  https://www.who.int/medicines/areas/quality_safety/quality_assurance/QAS16_686_rev_3_good_regulatory_practices_medical_products.pdf?ua=1